Biological sex differences in neurodegenerative diseases in Africa: a scoping review of evidence and research gaps.

Publication date: Jul 07, 2026

Biological sex is a well-established determinant of risk, progression, and therapeutic response in neurodegenerative diseases (NDs). However, current evidence on sex differences in NDs is from high-income Western populations. This review aims to map and synthesize evidence on biological sex differences in NDs in Africa, and to identify key research gaps. This scoping review was conducted in accordance with the Joanna Briggs Institute methodology and reported in accordance with the PRISMA-ScR guidelines. A literature search was conducted on PubMed, African Journals Online, Sabinet Journals, ScienceDirect, and Google Scholar. We included studies conducted in African countries that reported sex disaggregated data or examined biological sex differences in at least one ND. Data were synthesized descriptively. All included studies reported sex distribution, but most (about 84%) did so only descriptively. Approximately 17% conducted sex-stratified analyses beyond prevalence. Similar to global epidemiological trends, several studies suggested a higher prevalence or odds of dementia and multiple sclerosis among females, while male predominance was observed in Parkinson’s disease and Amyotrophic lateral sclerosis studies. An earlier onset and a higher mutation frequency in LRRK2-G2019S were reported in females with Parkinson’s disease in some studies, while another study reported a higher mortality rate in females with dementia. No study evaluated sex specific biomarker profiles, disease progression, or treatment response. Evidence on biological sex differences in NDs in Africa remains limited and is largely descriptive. Mechanistic, longitudinal, and biomarker-based investigations are largely absent.

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Concepts Keywords
Africa
Neurodegenerative disease
Sex differences
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Semantics

Type Source Name
disease MESH neurodegenerative diseases
pathway REACTOME Neurodegenerative Diseases
disease MESH included
disease MESH dementia
disease MESH multiple sclerosis
disease MESH Parkinson’s disease
disease MESH Amyotrophic lateral sclerosis
pathway KEGG Amyotrophic lateral sclerosis
disease MESH disease progression
pathway REACTOME Reproduction
drug DRUGBANK Coenzyme M
disease MESH neurological disorders
disease MESH death
disease MESH frontotemporal dementia
disease MESH motor neuron diseases
disease MESH Neurocognitive Disorders
disease MESH cognitive decline
drug DRUGBANK Factor IX Complex (Human)
disease MESH PCC
disease MESH HIV infection
pathway REACTOME HIV Infection
disease MESH injury
disease MESH neuroinflammation
disease MESH Alzheimer’s disease
disease MESH Huntington’s disease
disease MESH fatigue
disease MESH Lewy body dementia
disease MESH neurologic manifestations
disease MESH myelopathy
disease MESH movement disorders
disease MESH neuroleptic malignant syndrome
disease MESH secondary parkinsonism
disease MESH parkinsonism
disease MESH Tremor
disease MESH Bradykinesia
disease MESH Vascular Dementia
disease MESH Dis
disease MESH Syndromes
disease MESH AIDS
drug DRUGBANK Diethylstilbestrol
disease MESH des
drug DRUGBANK Levodopa
drug DRUGBANK Carbidopa
disease MESH MDS

Original Article

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